| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:44955237-44955437 | Common:2; Rare:65 | ||||
| chr19:44974321-44974594 | Common:1; Rare:78 | ||||
| chr19:45038943-45039124 | Rare:66 | ||||
| chr19:45079173-45079284 | Rare:29 | ||||
| chr19:45091488-45091796 | Common:2; Rare:87 | ||||
| chr19:45178168-45178365 | Common:1; Rare:71 | ||||
| chr19:45178626-45178816 | Common:4; Rare:45; Clinvar:1; Clinvar (benign):3 | ||||
| chr19:45251160-45251371 | Common:3; Rare:67 | ||||
| chr19:45263119-45263364 | Common:1; Rare:58 | ||||
| chr19:45370548-45370731 | Common:2; Rare:53 | ||||
| chr19:45406340-45406682 | Common:2; Rare:84 | ||||
| chr19:45423477-45423679 | Common:2; Rare:40; Clinvar (benign):1 | ||||
| chr19:45423816-45423992 | Common:2; Rare:37 | ||||
| chr19:45506549-45506629 | Common:1; Rare:24 | ||||
| chr19:45507228-45507586 | Common:1; Rare:96 |